Multi-function conducting elements for a catheter

Information

  • Patent Grant
  • 12042246
  • Patent Number
    12,042,246
  • Date Filed
    Friday, January 29, 2021
    3 years ago
  • Date Issued
    Tuesday, July 23, 2024
    4 months ago
Abstract
Described embodiments include an apparatus that includes an expandable structure, configured for insertion into a body of a subject, and a plurality of conducting elements coupled to the expandable structure. Each of the conducting elements comprises a respective coil and has an insulated portion that is electrically insulated from tissue of the subject, and an uninsulated portion configured to exchange signals with the tissue, while in contact with the tissue. Other embodiments are also described.
Description
FIELD OF THE INVENTION

Embodiments of the present invention relate generally to the field of medical devices, and particularly to catheters for recording intracardiac electrocardiogram (ECG) signals and/or ablating cardiac tissue.


BACKGROUND

In some applications, a basket catheter, comprising a large number of electrodes disposed on a plurality of splines, is used to acquire intracardiac electrocardiogram (ECG) signals. Such signals may be used, for example, to construct an electroanatomical map of the heart.


In other applications, a balloon catheter, comprising a plurality of electrodes disposed on a balloon, is used to ablate cardiac tissue, and/or to acquire intracardiac ECG signals.


US Patent Application Publication 2011/0118590, whose disclosure is incorporated herein by reference, describes an interventional system for internal anatomical examination that includes a catheterization device for internal anatomical insertion. The catheterization device includes at least one magnetic field sensor for generating an electrical signal in response to rotational movement of the at least one sensor about an axis through the catheterization device within a magnetic field applied externally to patient anatomy, and a signal interface for buffering the electrical signal for further processing. A signal processor processes the buffered electrical signal to derive a signal indicative of angle of rotation of the catheterization device relative to a reference. The angle of rotation is about an axis through the catheterization device. A reproduction device presents a user with data indicating the angle of rotation of the catheterization device.


US Patent Application Publication 2003/0093067, whose disclosure is incorporated herein by reference, describes systems and methods for imaging a body cavity and for guiding a treatment element within a body cavity. A system may include an imaging subsystem having an imaging device and an image processor that gather image data for the body cavity. A mapping subsystem may be provided, including a mapping device and a map processor, to identify target sites within the body cavity, and provide location data for the sites. The system may also include a location processor coupled to a location element on a treatment device to track the location of the location element. The location of a treatment element is determined by reference to the location element. A treatment subsystem including a treatment device having a treatment element and a treatment delivery source may also be provided. A registration subsystem receives and registers data from the other subsystems, and displays the data.


U.S. Pat. No. 6,272,371, whose disclosure is incorporated herein by reference, describes an invasive probe apparatus including a flexible elongate probe having a distal portion adjacent to a distal end thereof for insertion into the body of a subject, which portion assumes a predetermined curve form when a force is applied thereto. First and second sensors are fixed to the distal portion of the probe in known positions relative to the distal end, which sensors generate signals responsive to bending of the probe. Signal processing circuitry receives the bend responsive signals and processes them to find position and orientation coordinates of at least the first sensor, and to determine the locations of a plurality of points along the length of the distal portion of the probe.


US Patent Application Publication 2006/0025677, whose disclosure is incorporated herein by reference, describes a surgical navigation system for navigating a region of a patient that may include a non-invasive dynamic reference frame and/or fiducial marker, sensor tipped instruments, and isolator circuits. The dynamic reference frame may be placed on the patient in a precise location for guiding the instruments. The dynamic reference frames may be fixedly placed on the patient. Also the dynamic reference frames may be placed to allow generally natural movements of soft tissue relative to the dynamic reference frames. Also methods are provided to determine positions of the dynamic reference frames. Anatomical landmarks may be determined intra-operatively and without access to the anatomical structure.


U.S. Pat. No. 6,892,091, whose disclosure is incorporated herein by reference, describes an apparatus and method for rapidly generating an electrical map of a chamber of a heart that utilizes a catheter including a body having a proximal end and a distal end. The distal end has a distal tip and an array of non-contact electrodes having a proximal end and a distal end and at least one location sensor. Preferably, two location sensors are utilized. The first location sensor is preferably proximate to the catheter distal tip and the second location sensor is preferably proximate to the proximal end of the non-contact electrode array. The catheter distal end further preferably includes a contact electrode at its distal tip. Preferably, at least one and preferably both of the location sensors provide six degrees of location information. The location sensor is preferably an electromagnetic location sensor. The catheter is used for rapidly generating an electrical map of the heart within at least one cardiac cycle and preferably includes cardiac ablation and post-ablation validation.


SUMMARY OF THE INVENTION

There is provided, in accordance with some embodiments of the present invention, apparatus that includes an expandable structure, configured for insertion into a body of a subject, and a plurality of conducting elements coupled to the expandable structure. Each of the conducting elements includes a respective coil, and has an insulated portion that is electrically insulated from tissue of the subject, and an uninsulated portion configured to exchange signals with the tissue, while in contact with the tissue.


In some embodiments, the expandable structure includes a balloon.


In some embodiments, the expandable structure includes a basket.


In some embodiments, each of the conducting elements includes an electrode connected to the coil, the electrode being configured to exchange the signals with the tissue, and the coil being configured to carry the exchanged signals.


In some embodiments, the coil is situated proximally to the electrode to which the coil is connected.


In some embodiments, the coil is a single-loop coil.


In some embodiments, the coil is a helical coil.


In some embodiments, the coil is flat.


In some embodiments, the apparatus further includes two leads connected to each conducting element of the conducting elements, configured to carry the signals between the conducting element and a proximal end of the apparatus.


In some embodiments, at least part of each conducting element of the conducting elements has an electrical resistance that varies in response to strain to which the conducting element is subjected inside the body of the subject.


In some embodiments, each of the conducting elements includes a thermocouple junction.


In some embodiments, the coil includes the uninsulated portion.


There is further provided, in accordance with some embodiments of the present invention, a method that includes receiving from a conducting element, via two leads that connect the conducting element to a proximal end of a catheter, a voltage difference that was induced across the conducting element by a magnetic field. The method further includes, in response to the voltage difference, ascertaining a location of the conducting element, and, while the conducting element is in contact with tissue of a subject, exchanging a signal with the tissue via the conducting element and at least one of the leads.


In some embodiments, the signal is an electrocardiogram (ECG) signal, and exchanging the signal includes acquiring the ECG signal from the tissue.


In some embodiments, the signal is an ablation signal, and exchanging the signal includes passing the ablation signal into the tissue.


In some embodiments, exchanging the signal includes exchanging the signal while the conducting element is inside a body of a subject.


In some embodiments, the conducting element is a single-loop coil.


In some embodiments, the conducting element is a helical coil.


In some embodiments, the voltage difference is a first voltage difference, and the method further includes measuring a temperature, by measuring a second voltage difference across the leads.


In some embodiments, the method further includes measuring a strain exerted on the conducting element, by measuring an electrical resistance of the conducting element.


In some embodiments, the method further includes measuring an impedance between the conducting element and a patch coupled to skin of the subject, by passing an electric current between the conducting element and the patch, wherein the ascertaining of the location is further in response to the measured impedance.


The present invention will be more fully understood from the following detailed description of embodiments thereof, taken together with the drawings, in which:





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a schematic illustration of a basket catheter, in accordance with some embodiments of the present invention;



FIGS. 2-3 are schematic illustrations of circuitry for processing signals received from conducting elements, in accordance with some embodiments of the present invention; and



FIG. 4 is a schematic illustration of a catheter comprising multi-function conducting elements, in accordance with some embodiments of the present invention.





DETAILED DESCRIPTION OF EMBODIMENTS
Overview

Embodiments described herein include catheters comprising conducting elements that perform, e.g., simultaneously, a plurality of functions. For example, the conducting elements may function as electromagnetic sensors, by outputting, in the presence of a magnetic field, signals that may be used to ascertain the location and/or orientation of the catheter on which the conducting elements are disposed. In addition, the conducting elements may function as electrodes. For example, the conducting elements may be used to exchange signals with tissue, such as by acquiring ECG signals from tissue, or passing ablating signals into tissue. Alternatively or additionally, the conducting elements may be used to measure impedance, temperature, strain, and/or other relevant parameters.


More particularly, embodiments described herein include a basket catheter that may be used, for example, to build an electroanatomical map. The basket catheter comprises a plurality of splines at its distal end, and further comprises a plurality of helical conducting elements, which are disposed on the splines. During the electroanatomical mapping procedure, the helical conducting elements function as inductors, in that a generated magnetic field induces respective voltage differences across the conducting elements. Based on the induced voltage differences, the respective locations and orientations of the conducting elements—and hence, the location and orientation of the basket catheter—may be precisely determined.


The helical conducting elements additionally function as electrodes for acquiring ECG signals, such that it may not be necessary to equip the basket catheter with separate ECG-acquiring electrodes. For example, an electrically-insulative layer may cover the majority of each of the helical conducting elements, but leave a small portion of each of the helical conducting elements exposed. This exposed portion, when brought into contact with the intracardiac tissue, acquires ECG signals from the tissue.


The helical conducting elements described herein may thus function in two capacities—e.g., simultaneously—during a single procedure. First, they may function as ECG electrodes, by sensing the intracardiac ECG signals. Second, they may function as magnetic-field sensors, by outputting location-indicating signals (in the form of the above-described induced voltages) in response to the generated magnetic field. The conducting elements may thus be described as ECG electrodes that additionally function as magnetic-field sensors, or as magnetic-field sensors that additionally function as ECG electrodes. (Notwithstanding the above, in some embodiments, the conducting elements are used only as magnetic-field sensors, and separate electrodes coupled to the splines are used to acquire the ECG signals.)


Other embodiments described herein include a balloon catheter, comprising a balloon, and a plurality of conducting elements coupled to the balloon. Each one of the conducting elements comprises an electrode, configured to exchange signals with tissue, and a coil that is connected to the electrode. The coil carries the signals that are exchanged with the tissue, and also outputs signals (in the form of induced voltages) in response to a magnetic field. The conducting elements thus function as both magnetic-field sensors and as electrodes. Alternatively or additionally, the conducting elements may measure other parameters, such as impedance, temperature, or strain.


Embodiments described herein further include circuitry for processing signals received from the multi-function conducting elements. For example, the circuitry described herein may generate, based on signals received from the above-described helical conducting elements, a plurality of outputs, which are used by a processor to construct an electroanatomical map. These outputs include a plurality of first outputs, which indicate the electrical activity of the tissue, a plurality of second outputs, which indicate the respective induced voltage differences across the conducting elements, and a plurality of third outputs, which indicate the proximity to the tissue of each of the conducting elements.


Apparatus Description

Reference is initially made to FIG. 1, which is a schematic illustration of a basket catheter 22, in accordance with some embodiments of the present invention. FIG. 1 depicts a physician 34 using basket catheter 22 to perform an electroanatomical mapping of a heart 25 of a subject 26. During the mapping procedure, the distal end of the catheter, which comprises a basket 20 of splines 28, is inserted into heart 25. The splines are then brought into contact with the intracardiac tissue, and conducting elements 24 on the splines acquire intracardiac ECG signals. A console 36, which is connected to the basket catheter and comprises a computer processor 32, receives these ECG signals.


While the intracardiac ECG signals are being acquired, a magnetic field is generated by a plurality of magnetic-field generators 30 located underneath subject 26 or otherwise in the vicinity of the subject. (As shown in FIG. 1, a signal generator (“SIG GEN”) 40 in console 36 may cause generators 30 to generate the magnetic field by supplying an alternating current to the generators.) The magnetic field induces voltage differences across conducting elements 24. The induced voltage differences are received by the console, and, based on the induced voltages, processor 32 ascertains the position of each of the conducting elements. Processor 32 then constructs an electroanatomical map of the heart, based on the ECG signals (which indicate the electrical activity of the intracardiac tissue) and the voltages received from the helical conducting elements (which indicate the respective locations of the sources of the ECG signals). Such a map may be displayed on a monitor 38 for viewing by physician 34, and/or stored for later analysis.


Splines 28 may be arranged to define any suitably-shaped basket, such as the spheroidal basket shown in FIG. 1. FIG. 1 shows an embodiment in which a plurality of helical conducting elements 24 are disposed on the surface of each of the splines. The top-left portion of the figure shows an enlarged view of a single such helical conducting element. In this enlarged view, the solid portion of the conducting element corresponds to the portion of the conducting element that is on the near side of the spline, facing the viewer. The dotted portion corresponds to the portion of the conducting element that is on the far side of the spline, facing away from the viewer. Each of the two terminals of each of the conducting elements is typically connected to the console via a wire 42 which passes through the interior of the spline.


In some embodiments, the conducting elements are printed onto the splines. For example, each of the conducting elements may comprise electrically-conductive paint that is helically painted onto the splines. In other embodiments, the conducting elements comprise wires that are wound (i.e., coiled) around, and glued or otherwise attached to, the splines. In any case, for embodiments in which the helical conducting elements are on the surface of the splines, an electrically-insulative layer 44 typically covers at least a majority of each of the helical conducting elements. Electrically-insulative layer 44 prevents the turns of any given conducting element from being shorted with each other.


Typically, the electrically-insulative layer does not cover a portion of exactly one respective turn of each of the helical conducting elements. Thus, the electrically-insulative layer prevents shorting of the turns (in that no more than one turn of each conducting element is exposed), but also allows the conducting elements to acquire ECG signals. For example, the enlarged portion of FIG. 1 shows an embodiment in which the electrically-insulative layer exposes a portion 46 of the conducting element. Exposed portion 46 may be brought into contact with tissue, in order to acquire an ECG signal.


As noted above, the exposed portion of the conducting element is confined to one turn of the conducting element. This means that the distance between the distalmost exposed portion of the conducting element and the proximal most exposed portion of the conducting element is less than the distance D that separates between successive turns of the conducting element.


In some embodiments, the electrically-insulative layer is contiguous across a plurality of conducting elements. In other embodiments, as depicted in FIG. 1, the electrically-insulative layer is discontiguous, such that no portion of the electrically-insulative layer covers more than one of the conducting elements. Similarly, for any given conducting element, the cover provided by the electrically-insulative layer may be contiguous or discontiguous. As an example of the latter, in FIG. 1, the conducting element is covered by two separate, disjoint portions of the electrically-insulative layer, these portions being on respective opposite sides of exposed portion 46 of the conducting element.


In some embodiments, alternatively to being disposed on the splines as in FIG. 1, the conducting elements are contained within the splines. In such embodiments, the splines, being made of an electrically-insulative material (such as plastic), provide the “cover” that prevents the conducting elements from being shorted. For embodiments in which the conducting elements are additionally used to acquire ECG signals, the splines are shaped to define a plurality of openings that expose a portion of exactly one respective turn of each of the helical conducting elements. In other words, such embodiments are analogous to the embodiments described above, with the surface of the spline functioning analogously to electrically-insulative layer 44 in preventing shorting of the conducting elements, but also, optionally, providing for ECG-signal acquisition.


Reference is now made to FIG. 2, which is a schematic illustration of circuitry 48 for processing signals received from conducting elements 24, in accordance with some embodiments of the present invention. Circuitry 48 is typically located within console 36, between the catheter-console interface and the processor. As shown in FIG. 2, circuitry 48 is connected to each helical conducting element 24, typically via exactly two connections (or “leads”) connected to the conducting element: a first connection 50a to one terminal of the conducting element, and a second connection 50b to the other terminal of the conducting element. As further described below, circuitry 48 generates outputs based on signals received, via connections 50a and 50b, from each helical conducting element. Based on these outputs, processor 32 constructs an electroanatomical map of the subject's heart.


Typically, circuitry 48 comprises a first differential amplifier 52a and a second differential amplifier 52b. Connections 50a and 50b are connected to second differential amplifier 52b, while one of the connections—e.g., first connection 50a—is also connected to first differential amplifier 52a. Connections 50a and 50b thus carry inputs to the differential amplifiers, as further described below.


As described above, the exposed portion of each conducting element 24 is brought into contact with intracardiac tissue 56, such that an ECG voltage (referred to above as an “ECG signal”) is transferred to the conducting element from the tissue. (The ECG voltage is generally constant across the conducting element, i.e., the ECG voltage at the terminal of the conducting element is not significantly different from the ECG voltage at the exposed portion of the conducting element.) First connection 50a carries the ECG voltage to first differential amplifier 52a, which generates a first output 54a based on the ECG voltage, by amplifying a difference between the received ECG voltage and a reference voltage. The processor derives electrical-activity information from first output 54a, and uses this information to build the electroanatomical map. Typically, the reference voltage is the voltage at a reference electrode 58 disposed on the basket catheter, e.g., on a central spline of the catheter shaft (not shown in FIG. 1). (In FIG. 2, reference electrode 58 is connected to ground, such that the reference voltage is ground.)


Connection 50a also carries, to second differential amplifier 52b, the voltage induced by the magnetic field at one terminal of the conducting element, while connection 50b carries the voltage induced at the other terminal. In other words, connections 50a and 50b collectively carry, to the second differential amplifier, the voltage difference that is induced across the conducting element. Based on this voltage difference, second differential amplifier 52b generates a second output 54b, by amplifying the voltage difference. Second output 54b includes anatomical information, in that the second output indicates the position of the conducting element, and hence, the location of the source of the ECG signal. The processor derives this anatomical information from the second output, and then, in building the electroanatomical map, combines this anatomical information with the electrical-activity information derived from the first output.


Typically, circuitry 48 further comprises a current source, or, as in FIG. 2, a voltage source 60 in series with a resistor 62, which together function as a current source. The current source passes a current “I” over connection 50a and between the conducting element and reference electrode 58 (or a different reference electrode that is not used for the ECG reference voltage). During the passing of the current, the voltage on the conducting element indicates the impedance that is seen by the conducting element; the higher the voltage, the higher the impedance. The impedance, in turn, indicates the proximity of the conducting element to the tissue; the higher the impedance, the greater the proximity. Thus, the voltage on the conducting element indicates the proximity of the conducting element to the tissue. The first differential amplifier generates a third output 54c based on this proximity-indicating voltage, by amplifying the difference between the proximity-indicating voltage and the reference voltage. The processor then uses the third output to build the electroanatomical map. In particular, the processor first derives, from the third output, the proximity of the conducting element to the tissue. The processor then decides whether to accept the first (electrical-activity-related) output, based on the proximity. For example, the processor may compare the proximity to a threshold, and accept the first output only if the proximity is greater than the threshold (i.e., the distance between the conducting element and the tissue is sufficiently small).


It is noted that the ECG voltage, the induced voltage, and the proximity-indicating voltage are of sufficiently different frequencies, such that the three voltages may be simultaneously carried on connection 50a (and hence, simultaneously received by the circuitry). Thus, first output 54a, second output 54b, and third output 54c may be generated at the same time. In some embodiments, an adder 61 adds the first output, the second output, and the third output, yielding a combined output 64 having a plurality of components at various frequencies. Combined output 64 is then passed to an analog-to-digital converter (ADC) 66, which converts the combined output to a digital signal that is passed to the processor.


Although, for simplicity, only a single helical conducting element 24 is shown in FIG. 2, basket catheter 22 typically comprises a large number of helical conducting elements. On this note, reference is now made to FIG. 3, which is a schematic illustration of circuitry 48, in accordance with some embodiments of the present invention.



FIG. 3 shows a way in which the configuration of circuitry 48 shown in FIG. 2 may be extended to handle a large number of inputs from a large number of helical conducting elements. In particular, in FIG. 3, a block 68 of circuitry that is shown in FIG. 2 is replicated for each of the conducting elements. Thus, in FIG. 3, a conducting element 24a connects to a block 68a of circuitry, a conducting element 24b connects to a block 68b, and a conducting element 24c connects to a block 68c. Similarly, resistor 62 is replicated for each of the conducting elements, such that voltage source 60 may be connected to block 68a via a resistor 62a, to block 68b via a resistor 62b, or to block 68c via a resistor 62c. (Typically, switches 70 ensure that the voltage source is connected to no more than one block at a time.) Thus, for example, to pass a current between conducting element 24a and the reference electrode, the voltage source is connected to block 68a.


As indicated by the three-dot sequences in the figure, the configuration shown in FIG. 3 may be extended to handle any number of conducting elements.


It is emphasized that the principles described herein may be applied in many ways. For example, the scope of the present disclosure includes using each of one or more coils, and/or other conducting elements, for both (i) magnetic tracking, and (ii) exchanging signals with tissue, in any relevant application. (Circuitry described with reference to FIGS. 2-3 may be modified as appropriate to suit the application.) Exchanging signals with tissue includes, for example, acquiring ECG signals as described above, and/or passing ablating signals into tissue. (In the latter case, the same leads that carry the induced voltage from the conducting element may be used to deliver the ablating signal to the conducting element.) Moreover, the multi-function sensors described herein may be disposed on any suitable apparatus, including, for example, an intrabody device such as a lasso catheter, balloon catheter, or other type of catheter.


For example, reference is now made to FIG. 4, which is a schematic illustration of a catheter 72 comprising multi-function conducting elements 74, in accordance with some embodiments of the present invention. Catheter 72, which may be described as a “balloon catheter,” comprises a balloon 76, located at or near the distal end of the shaft 82 of the catheter, and a plurality of multi-function conducting elements coupled to balloon 76. Conducting elements 74 may, for example, be printed onto the surface of the balloon, or may be coupled to the balloon in any other suitable way.


In some embodiments, each conducting element 74 comprises an electrode 78, configured to exchange signals with tissue, and a coil 80 electrically connected to electrode 78. As opposed to coils 80, which are generally electrically insulated from the tissue, electrodes 78 are not insulated, such that the electrodes may make electrical contact with the tissue. Leads (or “connections”) 88, which run proximally-distally through shaft 82, connect the conducting elements to the proximal end of the catheter, which is connected to console 36 (FIG. 1). As shown in FIG. 4, catheter 72 may also comprise one or more additional electrodes 78, which are not coupled to coils, but instead, are coupled directly to leads 86.


Following the insertion of catheter 72 into the heart of a subject (as generally depicted in FIG. 1 for basket catheter 22), balloon 76 is inflated and one or more electrodes 78 are brought into contact with the intracardiac tissue. The electrodes then exchange signals with the tissue, e.g., by acquiring intracardiac ECG signals, and/or passing ablating signals into the tissue. Each such signal is carried to or from the relevant electrode by the coil and/or lead to which the electrode is attached. For example, in the case of an electrode belonging to a multi-function conducting element, each exchanged signal is carried between the conducting element and the proximal end of the catheter by a lead 88, and between the lead and the electrode by coil 80. (Coil 80 thus functions as a conductive trace.)


As shown in FIG. 4, leads 88 may be integrally formed with, and hence entirely continuous with, the coils, such that each coil may be described as the distal looped end of a single lead that runs distally through shaft 82, forms a loop along the surface of the balloon, and then returns, passing proximally, through the catheter shaft.


Coils 80 also output location-indicating signals in response to a magnetic field. In particular, in the presence of an externally-applied magnetic field, an alternating current (AC) voltage is induced in the coil, creating an AC voltage difference between the two terminals 92 of each coil, this voltage difference indicating the location and/or orientation of the coil relative to magnetic-field generators 30 (FIG. 1). For example, FIG. 4 shows an induced voltage difference V2−V1 between terminals 92 of one of the coils. This voltage difference is carried by leads 88 to the console. Processor 32 receives the voltage difference, and, in response to the voltage difference, ascertains the location and/or orientation of the coil (and hence, of the electrode to which the coil is connected).


(The “terminals” of the coil are the two points, at the proximal end of the coil, at which the coil becomes effectively closed, such that the coil meets, or “becomes,” leads 88. At the proximal end of the coil, leads 88 may be in mechanical (but not electrical) contact with one another, and, in some embodiments, may cross over one another.)


The location-indicating signals from the conducting elements may be used to guide the conducting elements to the appropriate location(s) for signal exchange. For example, while a particular conducting element is in contact with tissue, a location-indicating signal may be received from the conducting element. If the location indicated by the location-indicating signal is a desired location for signal exchange, a signal may be exchanged with the tissue via the conducting element (and in particular, the electrode belonging to the conducting element) and at least one of its leads. Otherwise, the position and/or orientation of catheter 72 may be adjusted as appropriate, prior to the signal exchange.


Each coil may be situated proximally or distally to the electrode to which the coil is connected. Typically, as shown, the coil is flat, i.e., it is not a barrel coil, such that the coil does not overly protrude from the surface of the balloon. Typically, as shown, each coil is a single-loop coil. In some embodiments, as shown, the coil is shaped to define a polygon, e.g., a five-sided polygon. Alternatively, the coil may have any other suitable shape, such as that of a circle or ellipse. As shown, the coil may be connected to the electrode (e.g., at the “base” of the polygon) by a connecting wire 90.


In some embodiments, each coil 80 also functions as an electrode. For example, each coil may comprise, in addition to an insulated portion that is electrically insulated from the tissue, an uninsulated portion. This uninsulated portion, while in contact with the tissue, exchanges signals, such as ECG signals and ablation signals, with the tissue. The coil thus performs at least three functions: (i) the exchange of signals with the tissue, (ii) the carrying of these signals to or from the tissue, and (iii) the output of voltage differences in response to a magnetic field. It is noted that a conducting element 74 that comprises such a coil does not necessarily comprise an electrode 78 that is separate from the coil, since the coil may already perform the function of electrode 78.


In some embodiments, at least part of each of the conducting elements has an electrical resistance that varies in response to strain to which the conducting element is subjected inside the body of the subject. For example, coil 80, in whole or in part, may be made of a biocompatible strain-sensitive material, and/or may have a form that renders the coil sensitive to strain. In such embodiments, the strain exerted on each of the conducting elements may be measured, by measuring the electrical resistance of the conducting elements. For example, a current of known amplitude (and a frequency different from that of the generated magnetic field) may be passed through each of the conducting elements via the leads connected thereto, and the resulting voltage between the proximal terminals of the leads may be measured. This voltage, divided by the amplitude of the current (and taking into account the electrical resistance of the leads), gives the electrical resistance of the conducting element, which in turn indicates the magnitude of the strain applied to the conducting element. The strain applied to the catheter may then be derived from the strains that were measured for the conducting elements.


Alternatively or additionally, each of the conducting elements may comprise a thermocouple junction. In other words, each of the conducting elements may comprise two portions, made of different metals, connected to one another at a temperature-sensing junction, such that each of the conducting elements functions as a thermocouple temperature sensor. For example, a portion of coil 80 may be made of copper, and another portion of the coil may be made of constantan, the copper and constantan being connected to one another at a thermocouple junction. Such a junction may be located, for example, at the distal end of coil 80, e.g., at the point at which coil 80 meets connecting wire 90. Alternatively, such a junction may be located anywhere else along coil 80, or along one of leads 88. In such embodiments, a thermocouple junction may be used to measure the temperature of the tissue and/or of the ambient environment. For example, while a thermocouple junction is contacting the subject's tissue, the temperature of the tissue may be measured, by measuring the voltage difference across the leads. (This voltage is a direct current (DC) voltage, such that it may be differentiated from the alternating voltage induced by the generated magnetic field.)


Alternatively or additionally, an electric current may be passed between the conducting element and a patch coupled to skin of the subject, such as to measure the impedance between the conducting element and the patch. Such an impedance measurement may be used, for example, for an impedance-based tracking system, whereby the location of the conducting element is ascertained in response to the measured impedance, alternatively or additionally to being ascertained in response to the voltage induced in the conducting element by a generated magnetic field.


It is noted that the above-described strain, temperature, and impedance measurements may also be performed by conducting elements 24, described above with respect to FIG. 1, as well as by any other suitable multi-function conducting elements. The multi-function conducting elements described herein may be coupled to an expandable structure, such as basket 20 of FIG. 1 or balloon 76 of FIG. 4, or to any other suitable tool.


It will be appreciated by persons skilled in the art that the present invention is not limited to what has been particularly shown and described hereinabove. Rather, the scope of embodiments of the present invention includes both combinations and subcombinations of the various features described hereinabove, as well as variations and modifications thereof that are not in the prior art, which would occur to persons skilled in the art upon reading the foregoing description. Documents incorporated by reference in the present patent application are to be considered an integral part of the application except that to the extent any terms are defined in these incorporated documents in a manner that conflicts with the definitions made explicitly or implicitly in the present specification, only the definitions in the present specification should be considered.

Claims
  • 1. An apparatus, comprising: (a) an expandable structure extending along a longitudinal axis, configured for insertion into a body of a subject; and(b) a plurality of conducting elements disposed on a surface of the expandable structure, each of the plurality of conducting elements comprising a respective coil having two terminals, each of the coils is configured to induce an alternating current (AC) voltage difference between the two terminals in response to an external magnetic field, each of the coils including:i) an insulated portion of the coil electrically insulated from tissue of the subject, andii) an uninsulated portion of the coil connected electrically to the two terminals, the uninsulated portion configured to exchange signals with the tissue of the subject while in contact with the tissue of the subject.
  • 2. The apparatus according to claim 1, wherein the uninsulated portion comprises an electrode to pass ablating signals into the tissue.
  • 3. The apparatus according to claim 1, wherein the uninsulated portion comprises an electrode to acquire ECG signals from the tissue.
  • 4. The apparatus of claim 1, wherein the expandable structure comprises a balloon.
  • 5. The apparatus according to claim 1, wherein the expandable structure comprises a basket, the basket includes a plurality of splines configured to expand into a generally spheroidal structure such that each spline defines a portion of the surface of the expandable structure.
  • 6. The apparatus according to claim 1, further comprising a separate electrode connected to the coil, the electrode being configured to exchange the signals with the tissue, and the coil being configured to carry the exchanged signals from the electrode.
  • 7. The apparatus according to claim 6, wherein the coil is situated proximally to the conducting elements to which the coil is connected.
  • 8. The apparatus according to claim 1, wherein the coil comprises a single-loop coil.
  • 9. The apparatus according to claim 1, wherein the coil comprises a helical coil.
  • 10. The apparatus according to claim 1, wherein the coil comprises a generally flat coil disposed on a generally spherical surface of the expandable structure.
  • 11. A system, comprising: (a) an expandable structure, configured for insertion into a body of a subject; and(b) a plurality of conducting elements disposed on a surface of the expandable structure, each of the plurality of conducting elements comprising a respective coil having two terminals, each of the coils is configured to induce an alternating current (AC) voltage difference between the two terminals in response to an external magnetic field, each of the coils having:i) an insulated portion of the coil electrically insulated from tissue of the subject, andii) an uninsulated portion of the coil connected electrically to the two terminals, the uninsulated portion configured to exchange signals with the tissue of the subject while in contact with the tissue of the subject; and(c) a processor, the processor configured to:i) receive the exchanged signals from the uninsulated portion; andii) receive an output of the AC voltage difference between the two terminals in response to the external magnetic field.
  • 12. The system according to claim 11, wherein at least part of each conducting element of the conducting elements has an electrical resistance that varies in response to strain to which the conducting element is subjected inside the body of the subject.
  • 13. The system according to claim 11, wherein each of the conducting elements comprises a thermocouple junction.
  • 14. The system according to claim 11, wherein the processor is configured to measure a second voltage difference representative of temperature across the two terminals.
  • 15. The system of claim 11, wherein the processor is configured to measure an impedance between each of the conducting elements and a patch coupled to skin of the subject via an electric current provided between the conducting elements and the patch.
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuing application under 35 USC § 120 and claims the benefits of prior U.S. patent application Ser. No. 15/359,838 filed Nov. 23, 2016, now allowed, which prior application is a continuation-in-part of, and claims the benefit of, U.S. patent application Ser. No. 15/177,775, entitled “Dual-function sensors for a basket catheter,” filed Jun. 9, 2016, whose disclosure is incorporated herein by reference.

US Referenced Citations (686)
Number Name Date Kind
D123782 Paul Dec 1940 S
3316896 Louis May 1967 A
4276874 Wolvek et al. Jul 1981 A
4587975 Salo et al. May 1986 A
4699147 Chilson et al. Oct 1987 A
4709698 Johnston et al. Dec 1987 A
4805621 Heinze et al. Feb 1989 A
4940064 Desai Jul 1990 A
5178957 Kolpe et al. Jan 1993 A
5215103 Desai Jun 1993 A
5255679 Imran Oct 1993 A
5293869 Edwards et al. Mar 1994 A
5309910 Edwards et al. May 1994 A
5313943 Houser et al. May 1994 A
5324284 Imran Jun 1994 A
5345936 Pomeranz et al. Sep 1994 A
5365926 Desai Nov 1994 A
5396887 Imran Mar 1995 A
5400783 Pomeranz et al. Mar 1995 A
5411025 Webster, Jr. May 1995 A
5415166 Imran May 1995 A
5429617 Hammersmark et al. Jul 1995 A
5456254 Pietroski et al. Oct 1995 A
5465717 Imran et al. Nov 1995 A
5476495 Kordis et al. Dec 1995 A
5499981 Kordis Mar 1996 A
5505730 Edwards Apr 1996 A
5526810 Wang Jun 1996 A
5546940 Panescu et al. Aug 1996 A
5549108 Edwards et al. Aug 1996 A
5558073 Pomeranz et al. Sep 1996 A
5577509 Panescu et al. Nov 1996 A
5582609 Swanson et al. Dec 1996 A
5584830 Ladd et al. Dec 1996 A
5595183 Swanson et al. Jan 1997 A
5598848 Swanson et al. Feb 1997 A
5609157 Panescu et al. Mar 1997 A
5628313 Webster, Jr. May 1997 A
5681280 Rusk et al. Oct 1997 A
5702386 Stern et al. Dec 1997 A
5718241 Ben-Haim et al. Feb 1998 A
5722401 Pietroski et al. Mar 1998 A
5722403 McGee et al. Mar 1998 A
5725525 Kordis Mar 1998 A
5730128 Pomeranz et al. Mar 1998 A
5772590 Webster, Jr. Jun 1998 A
5782899 Imran Jul 1998 A
5797903 Swanson et al. Aug 1998 A
5823189 Kordis Oct 1998 A
5860974 Abele Jan 1999 A
5881727 Edwards Mar 1999 A
5893847 Kordis Apr 1999 A
5904680 Kordis et al. May 1999 A
5911739 Kordis et al. Jun 1999 A
5928228 Kordis et al. Jul 1999 A
5968040 Swanson et al. Oct 1999 A
5971983 Lesh Oct 1999 A
6012457 Lesh Jan 2000 A
6014579 Pomeranz et al. Jan 2000 A
6014590 Whayne et al. Jan 2000 A
6024740 Lesh et al. Feb 2000 A
6042580 Simpson Mar 2000 A
6050267 Nardella et al. Apr 2000 A
6070094 Swanson et al. May 2000 A
6119030 Morency Sep 2000 A
6123718 Tu et al. Sep 2000 A
6142993 Whayne et al. Nov 2000 A
6164283 Lesh Dec 2000 A
6171275 Webster, Jr. Jan 2001 B1
6176832 Habu et al. Jan 2001 B1
6198974 Webster, Jr. Mar 2001 B1
6216043 Swanson et al. Apr 2001 B1
6216044 Kordis Apr 2001 B1
6226542 Reisfeld May 2001 B1
6233491 Kordis et al. May 2001 B1
6272371 Shlomo Aug 2001 B1
6301496 Reisfeld Oct 2001 B1
6322558 Taylor et al. Nov 2001 B1
6332880 Yang et al. Dec 2001 B1
6380957 Banning Apr 2002 B1
6402740 Ellis et al. Jun 2002 B1
6428537 Swanson et al. Aug 2002 B1
D462389 Provence et al. Sep 2002 S
6456864 Swanson et al. Sep 2002 B1
6471693 Carroll et al. Oct 2002 B1
6511478 Burnside et al. Jan 2003 B1
6522930 Schaer et al. Feb 2003 B1
6569160 Goldin et al. May 2003 B1
6574492 Ben-Haim et al. Jun 2003 B1
6584345 Govari Jun 2003 B2
6600948 Ben-Haim et al. Jul 2003 B2
6656174 Hegde et al. Dec 2003 B1
6735465 Panescu May 2004 B2
6738655 Sen et al. May 2004 B1
6741878 Fuimaono et al. May 2004 B2
6748255 Fuimaono et al. Jun 2004 B2
6780183 Jimenez, Jr. et al. Aug 2004 B2
6785571 Glossop Aug 2004 B2
6814733 Schwartz et al. Nov 2004 B2
6837886 Collins et al. Jan 2005 B2
6866662 Fuimaono et al. Mar 2005 B2
6892091 Ben-Haim et al. May 2005 B1
6893433 Lentz May 2005 B2
6970730 Fuimaono et al. Nov 2005 B2
6973340 Fuimaono et al. Dec 2005 B2
6980858 Fuimaono et al. Dec 2005 B2
6986744 Krivitski Jan 2006 B1
6987995 Drysen Jan 2006 B2
6997924 Schwartz et al. Feb 2006 B2
7048734 Fleischman et al. May 2006 B1
7142903 Rodriguez et al. Nov 2006 B2
7149563 Fuimaono et al. Dec 2006 B2
7156816 Schwartz et al. Jan 2007 B2
7255695 Falwell et al. Aug 2007 B2
7257434 Fuimaono et al. Aug 2007 B2
7274957 Drysen Sep 2007 B2
7340307 Maguire et al. Mar 2008 B2
7377906 Selkee May 2008 B2
7399299 Daniel et al. Jul 2008 B2
7410486 Fuimaono et al. Aug 2008 B2
7442190 Abbound et al. Oct 2008 B2
7522950 Fuimaono et al. Apr 2009 B2
7536218 Govari et al. May 2009 B2
7591799 Selkee Sep 2009 B2
7593760 Rodriguez et al. Sep 2009 B2
7697972 Verard et al. Apr 2010 B2
RE41334 Beatty et al. May 2010 E
7720517 Drysen May 2010 B2
7756576 Levin Jul 2010 B2
7842031 Abboud et al. Nov 2010 B2
7846157 Kozel Dec 2010 B2
7853302 Rodriguez et al. Dec 2010 B2
7930018 Harlev et al. Apr 2011 B2
8000765 Rodriguez et al. Aug 2011 B2
8007495 McDaniel et al. Aug 2011 B2
8021327 Selkee Sep 2011 B2
8048032 Root et al. Nov 2011 B2
8048063 Aeby et al. Nov 2011 B2
8097926 De Graff et al. Jan 2012 B2
8103327 Harlev et al. Jan 2012 B2
8167845 Wang et al. May 2012 B2
8224416 De La Rama et al. Jul 2012 B2
8231617 Satake Jul 2012 B2
8235988 Davis et al. Aug 2012 B2
8267932 Baxter et al. Sep 2012 B2
8275440 Rodriguez et al. Sep 2012 B2
8346339 Kordis et al. Jan 2013 B2
8348888 Selkee Jan 2013 B2
8357152 Govari et al. Jan 2013 B2
D682289 DiJulio et al. May 2013 S
D682291 Baek et al. May 2013 S
8435232 Aeby et al. May 2013 B2
8447377 Harlev et al. May 2013 B2
8498686 Grunewald Jul 2013 B2
8517999 Pappone et al. Aug 2013 B2
D690318 Kluttz et al. Sep 2013 S
8545490 Mihajlovic et al. Oct 2013 B2
8560086 Just et al. Oct 2013 B2
8567265 Aeby et al. Oct 2013 B2
D694652 Tompkin Dec 2013 S
8641709 Sauvageau et al. Feb 2014 B2
8712550 Grunewald Apr 2014 B2
8721590 Seward et al. May 2014 B2
8755861 Harlev et al. Jun 2014 B2
8777161 Pollock et al. Jul 2014 B2
8825130 Just et al. Sep 2014 B2
D716340 Bresin et al. Oct 2014 S
8852181 Malecki et al. Oct 2014 B2
8906011 Gelbart et al. Dec 2014 B2
8918184 Torgerson et al. Dec 2014 B1
D720766 Mandal et al. Jan 2015 S
D721379 Moon et al. Jan 2015 S
8945120 McDaniel et al. Feb 2015 B2
D724618 Shin Mar 2015 S
8979839 De La Rama et al. Mar 2015 B2
8998893 Avitall Apr 2015 B2
D729263 Ahn et al. May 2015 S
9037264 Just et al. May 2015 B2
9060756 Bencini et al. Jun 2015 B2
9089350 Willard Jul 2015 B2
D736780 Wang Aug 2015 S
9126023 Sahatjian et al. Sep 2015 B1
9131980 Bloom Sep 2015 B2
D740308 Kim et al. Oct 2015 S
D743424 Danielyan et al. Nov 2015 S
D744000 Villamor et al. Nov 2015 S
9173758 Brister et al. Nov 2015 B2
9179963 Ben-Ezra et al. Nov 2015 B2
9204929 Solis Dec 2015 B2
D747742 Fan et al. Jan 2016 S
D750644 Bhutani et al. Mar 2016 S
9277960 Weinkam et al. Mar 2016 B2
9283034 Katoh et al. Mar 2016 B2
9289141 Lowery et al. Mar 2016 B2
D753690 Vazquez et al. Apr 2016 S
9314208 Altmann et al. Apr 2016 B1
9320631 Moore et al. Apr 2016 B2
9339331 Tegg et al. May 2016 B2
9345540 Mallin et al. May 2016 B2
D759673 Looney et al. Jun 2016 S
D759675 Looney et al. Jun 2016 S
D764500 Wang Aug 2016 S
D765709 Gagnier Sep 2016 S
D767616 Jones et al. Sep 2016 S
D768696 Gagnier Oct 2016 S
9486282 Solis Nov 2016 B2
9554718 Bar-Tal et al. Jan 2017 B2
D782686 Werneth et al. Mar 2017 S
9585588 Marecki et al. Mar 2017 B2
9597036 Aeby et al. Mar 2017 B2
D783037 Hariharan et al. Apr 2017 S
9655677 Salahieh et al. May 2017 B2
9687297 Just et al. Jun 2017 B2
D791805 Segars Jul 2017 S
9693733 Altmann et al. Jul 2017 B2
9782099 Williams et al. Oct 2017 B2
9788895 Solis Oct 2017 B2
9795442 Salahieh et al. Oct 2017 B2
9801681 Laske et al. Oct 2017 B2
9814618 Nguyen et al. Nov 2017 B2
9833161 Govari Dec 2017 B2
9894756 Weinkam et al. Feb 2018 B2
9895073 Solis Feb 2018 B2
9907609 Cao et al. Mar 2018 B2
9907610 Beeckler et al. Mar 2018 B2
9956035 Govari et al. May 2018 B2
9974460 Wu et al. May 2018 B2
9986949 Govari et al. Jun 2018 B2
9993160 Salvestro et al. Jun 2018 B2
10014607 Govari et al. Jul 2018 B1
10028376 Weinkam et al. Jul 2018 B2
10034637 Harlev et al. Jul 2018 B2
10039494 Altmann et al. Aug 2018 B2
10045707 Govari Aug 2018 B2
10078713 Auerbach et al. Sep 2018 B2
10111623 Jung et al. Oct 2018 B2
10130420 Basu et al. Nov 2018 B2
10136828 Houben et al. Nov 2018 B2
10143394 Solis Dec 2018 B2
10172536 Maskara et al. Jan 2019 B2
10182762 Just et al. Jan 2019 B2
10194818 Williams et al. Feb 2019 B2
10201311 Chou et al. Feb 2019 B2
10219860 Harlev et al. Mar 2019 B2
10219861 Just et al. Mar 2019 B2
10231328 Weinkam et al. Mar 2019 B2
10238309 Bar-Tal et al. Mar 2019 B2
10278590 Salvestro et al. May 2019 B2
D851774 Werneth et al. Jun 2019 S
10314505 Williams et al. Jun 2019 B2
10314507 Govari et al. Jun 2019 B2
10314648 Ge et al. Jun 2019 B2
10314649 Bakos et al. Jun 2019 B2
10349855 Zeidan et al. Jul 2019 B2
10350003 Weinkam et al. Jul 2019 B2
10362991 Tran et al. Jul 2019 B2
10375827 Weinkam et al. Aug 2019 B2
10376170 Quinn et al. Aug 2019 B2
10376221 Iyun et al. Aug 2019 B2
10398348 Osadchy et al. Sep 2019 B2
10403053 Katz et al. Sep 2019 B2
D861717 Brekke et al. Oct 2019 S
10441188 Katz et al. Oct 2019 B2
10470682 Deno et al. Nov 2019 B2
10470714 Altmann et al. Nov 2019 B2
10482198 Auerbach et al. Nov 2019 B2
10492857 Guggenberger et al. Dec 2019 B2
10542620 Weinkam et al. Jan 2020 B2
10575743 Basu et al. Mar 2020 B2
10575745 Solis Mar 2020 B2
10582871 Williams et al. Mar 2020 B2
10582894 Ben Zrihem et al. Mar 2020 B2
10596346 Aeby et al. Mar 2020 B2
10602947 Govari et al. Mar 2020 B2
10617867 Viswanathan et al. Apr 2020 B2
10660702 Viswanathan et al. May 2020 B2
10667753 Werneth et al. Jun 2020 B2
10674929 Houben et al. Jun 2020 B2
10681805 Weinkam et al. Jun 2020 B2
10682181 Cohen et al. Jun 2020 B2
10687892 Long et al. Jun 2020 B2
10688278 Beeckler et al. Jun 2020 B2
10702178 Dahlen et al. Jul 2020 B2
10716477 Salvestro et al. Jul 2020 B2
10758304 Aujla Sep 2020 B2
10765371 Hayam et al. Sep 2020 B2
10772566 Aujila Sep 2020 B2
10799281 Goertzen et al. Oct 2020 B2
10842558 Harlev et al. Nov 2020 B2
10842561 Viswanathan et al. Nov 2020 B2
10863914 Govari et al. Dec 2020 B2
10881376 Shemesh et al. Jan 2021 B2
10898139 Guta et al. Jan 2021 B2
10905329 Bar-Tal et al. Feb 2021 B2
10912484 Ziv-Ari et al. Feb 2021 B2
10918306 Govari et al. Feb 2021 B2
10939871 Altmann et al. Mar 2021 B2
10952795 Cohen et al. Mar 2021 B2
10973426 Williams et al. Apr 2021 B2
10973461 Baram et al. Apr 2021 B2
10987045 Basu et al. Apr 2021 B2
11006902 Bonyak et al. May 2021 B1
11040208 Govari et al. Jun 2021 B1
11045628 Beeckler et al. Jun 2021 B2
11051877 Sliwa et al. Jul 2021 B2
11109788 Rottmann et al. Sep 2021 B2
11116435 Urman et al. Sep 2021 B2
11129574 Cohen et al. Sep 2021 B2
11160482 Solis Nov 2021 B2
11164371 Yellin et al. Nov 2021 B2
20010031961 Hooven Oct 2001 A1
20020002369 Hood Jan 2002 A1
20020065455 Ben-Haim et al. May 2002 A1
20020068931 Wong et al. Jun 2002 A1
20020077627 Johnson et al. Jun 2002 A1
20020111618 Stewart et al. Aug 2002 A1
20020160134 Ogushi et al. Oct 2002 A1
20030018327 Truckai et al. Jan 2003 A1
20030028183 Sanchez et al. Feb 2003 A1
20030050637 Maguire et al. Mar 2003 A1
20030060820 Maguire et al. Mar 2003 A1
20030093067 Panescu May 2003 A1
20030144658 Schwartz et al. Jul 2003 A1
20040122445 Butler et al. Jun 2004 A1
20040147920 Keidar Jul 2004 A1
20040210121 Fuimaono et al. Oct 2004 A1
20040225285 Gibson Nov 2004 A1
20050033135 Govari Feb 2005 A1
20050070887 Taimisto et al. Mar 2005 A1
20050119686 Clubb Jun 2005 A1
20060009689 Fuimaono et al. Jan 2006 A1
20060009690 Fuimaono et al. Jan 2006 A1
20060013595 Trezza et al. Jan 2006 A1
20060025677 Verard et al. Feb 2006 A1
20060089637 Werneth et al. Apr 2006 A1
20060100669 Fuimaono et al. May 2006 A1
20060106375 Werneth et al. May 2006 A1
20060135953 Kania et al. Jun 2006 A1
20070071792 Varner et al. Mar 2007 A1
20070080322 Walba Apr 2007 A1
20070083194 Kunis et al. Apr 2007 A1
20070093806 Desai et al. Apr 2007 A1
20070276212 Fuimaono et al. Nov 2007 A1
20070287994 Patel Dec 2007 A1
20080018891 Hell et al. Jan 2008 A1
20080021313 Eidenschink et al. Jan 2008 A1
20080039790 Hasebe Feb 2008 A1
20080051707 Phan et al. Feb 2008 A1
20080140072 Stangenes et al. Jun 2008 A1
20080183132 Davies et al. Jul 2008 A1
20080188912 Stone et al. Aug 2008 A1
20080202637 Hector et al. Aug 2008 A1
20080208186 Slater Aug 2008 A1
20080234564 Beatty et al. Sep 2008 A1
20080249463 Pappone et al. Oct 2008 A1
20080262489 Steinke Oct 2008 A1
20080281312 Werneth et al. Nov 2008 A1
20090163890 Clifford et al. Jun 2009 A1
20090182318 Abboud et al. Jul 2009 A1
20090221907 Bar-Tal Sep 2009 A1
20090270850 Zhou et al. Oct 2009 A1
20100069836 Satake Mar 2010 A1
20100114269 Wittenberger et al. May 2010 A1
20100204560 Salahieh et al. Aug 2010 A1
20100222664 Lemon et al. Sep 2010 A1
20100234746 Sebelius Sep 2010 A1
20100256629 Wylie et al. Oct 2010 A1
20100324552 Kauphusman et al. Dec 2010 A1
20110004087 Fish et al. Jan 2011 A1
20110028848 Shaquer et al. Feb 2011 A1
20110118590 Zhang May 2011 A1
20110118632 Sinelnikov et al. May 2011 A1
20110118726 De La Rama et al. May 2011 A1
20110130648 Beeckler et al. Jun 2011 A1
20110160574 Harlev et al. Jun 2011 A1
20110190625 Harlev et al. Aug 2011 A1
20110245756 Arora et al. Oct 2011 A1
20110264000 Paul et al. Oct 2011 A1
20110282338 Fojtik Nov 2011 A1
20110295248 Wallace et al. Dec 2011 A1
20110301587 Deem et al. Dec 2011 A1
20110301597 McDaniel et al. Dec 2011 A1
20110313286 Whayne et al. Dec 2011 A1
20120017923 Sobe Jan 2012 A1
20120019107 Gabl et al. Jan 2012 A1
20120029511 Smith et al. Feb 2012 A1
20120065503 Rogers et al. Mar 2012 A1
20120071870 Salahieh et al. Mar 2012 A1
20120079427 Carmichael et al. Mar 2012 A1
20120101413 Beetel et al. Apr 2012 A1
20120101538 Ballakur et al. Apr 2012 A1
20120130229 Zellers et al. May 2012 A1
20120143177 Avitall Jun 2012 A1
20120143293 Mauch et al. Jun 2012 A1
20120172761 Meller et al. Jul 2012 A1
20120191079 Moll et al. Jul 2012 A1
20120197100 Razavi et al. Aug 2012 A1
20120209260 Lambert et al. Aug 2012 A1
20120323235 Danek et al. Dec 2012 A1
20130085360 Grunewald Apr 2013 A1
20130090649 Smith et al. Apr 2013 A1
20130090651 Smith Apr 2013 A1
20130109982 Sato et al. May 2013 A1
20130150693 D'Angelo et al. Jun 2013 A1
20130165916 Mathur et al. Jun 2013 A1
20130165941 Murphy Jun 2013 A1
20130165990 Mathur et al. Jun 2013 A1
20130169624 Bourier et al. Jul 2013 A1
20130172872 Subramaniam et al. Jul 2013 A1
20130172883 Lopes et al. Jul 2013 A1
20130178850 Lopes et al. Jul 2013 A1
20130190587 Lopes et al. Jul 2013 A1
20130261692 Cardinal et al. Oct 2013 A1
20130274562 Ghaffari et al. Oct 2013 A1
20130274658 Steinke et al. Oct 2013 A1
20130281813 Markowitz et al. Oct 2013 A1
20130281997 Davie Oct 2013 A1
20130282084 Mathur et al. Oct 2013 A1
20130296679 Condie et al. Nov 2013 A1
20130296852 Madjarov et al. Nov 2013 A1
20130318439 Landis et al. Nov 2013 A1
20140012242 Lee et al. Jan 2014 A1
20140018788 Engelman et al. Jan 2014 A1
20140025069 Willard et al. Jan 2014 A1
20140031813 Tellio et al. Jan 2014 A1
20140051968 Isham et al. Feb 2014 A1
20140052118 Laske et al. Feb 2014 A1
20140058197 Salahieh et al. Feb 2014 A1
20140058371 Krishnan Feb 2014 A1
20140107453 Maskara et al. Apr 2014 A1
20140121470 Scharf et al. May 2014 A1
20140148805 Stewart et al. May 2014 A1
20140180147 Thakur et al. Jun 2014 A1
20140180151 Maskara et al. Jun 2014 A1
20140180152 Maskara et al. Jun 2014 A1
20140227437 DeBoer et al. Aug 2014 A1
20140228838 Kirschenman Aug 2014 A1
20140243821 Salahieh et al. Aug 2014 A1
20140257069 Eliason et al. Sep 2014 A1
20140275993 Ballakur Sep 2014 A1
20140276712 Mallin et al. Sep 2014 A1
20140276756 Hill Sep 2014 A1
20140276811 Koblish et al. Sep 2014 A1
20140288546 Sherman et al. Sep 2014 A1
20140309512 Govari et al. Oct 2014 A1
20140330266 Thompson et al. Nov 2014 A1
20140357956 Salahieh et al. Dec 2014 A1
20150005799 Lindquist et al. Jan 2015 A1
20150011991 Buysman et al. Jan 2015 A1
20150025532 Hanson et al. Jan 2015 A1
20150025533 Groff et al. Jan 2015 A1
20150045863 Litscher et al. Feb 2015 A1
20150057519 Ben-David et al. Feb 2015 A1
20150057655 Osypka Feb 2015 A1
20150067512 Roswell Mar 2015 A1
20150080693 Solis Mar 2015 A1
20150080883 Haverkost et al. Mar 2015 A1
20150105770 Amit Apr 2015 A1
20150105774 Lindquist et al. Apr 2015 A1
20150112256 Byrne et al. Apr 2015 A1
20150112321 Cadouri Apr 2015 A1
20150119670 Madjarov et al. Apr 2015 A1
20150119875 Fischell et al. Apr 2015 A1
20150119878 Heisel et al. Apr 2015 A1
20150133919 McDaniel et al. May 2015 A1
20150141982 Lee May 2015 A1
20150157382 Avitall et al. Jun 2015 A1
20150157391 Ben-Ezra et al. Jun 2015 A1
20150208942 Bar-Tal et al. Jul 2015 A1
20150216591 Cao et al. Aug 2015 A1
20150216650 Shaltis Aug 2015 A1
20150238275 Kung et al. Aug 2015 A1
20150250424 Govari et al. Sep 2015 A1
20150265329 Lalonde et al. Sep 2015 A1
20150265339 Lindquist et al. Sep 2015 A1
20150265812 Lalonde Sep 2015 A1
20150270634 Buesseler et al. Sep 2015 A1
20150272667 Govari et al. Oct 2015 A1
20150327805 Ben-Haim Nov 2015 A1
20150327921 Govari et al. Nov 2015 A1
20150341752 Flynn Nov 2015 A1
20150342532 Basu et al. Dec 2015 A1
20150366608 Weber et al. Dec 2015 A1
20160000499 Lennox et al. Jan 2016 A1
20160038053 Bohorquez et al. Feb 2016 A1
20160051321 Salahieh et al. Feb 2016 A1
20160081746 Solis Mar 2016 A1
20160085431 Kim et al. Mar 2016 A1
20160106499 Ogata et al. Apr 2016 A1
20160113582 Altmann et al. Apr 2016 A1
20160113709 Maor Apr 2016 A1
20160166306 Pageard Jun 2016 A1
20160175041 Govari et al. Jun 2016 A1
20160183877 Williams et al. Jun 2016 A1
20160196635 Cho et al. Jul 2016 A1
20160228023 Govari Aug 2016 A1
20160228062 Altmann et al. Aug 2016 A1
20160256305 Longo et al. Sep 2016 A1
20160278853 Ogle et al. Sep 2016 A1
20160302858 Bencini Oct 2016 A1
20160338770 Bar-Tal et al. Nov 2016 A1
20160374748 Salahieh et al. Dec 2016 A9
20170027638 Solis Feb 2017 A1
20170042614 Salahieh et al. Feb 2017 A1
20170042615 Salahieh et al. Feb 2017 A1
20170065227 Marrs et al. Mar 2017 A1
20170071543 Basu et al. Mar 2017 A1
20170071544 Basu et al. Mar 2017 A1
20170071665 Solis Mar 2017 A1
20170080192 Giasolli et al. Mar 2017 A1
20170095173 Bar-Tal et al. Apr 2017 A1
20170100187 Basu et al. Apr 2017 A1
20170143227 Marecki et al. May 2017 A1
20170143359 Nguyen et al. May 2017 A1
20170156790 Aujla Jun 2017 A1
20170164464 Weinkam et al. Jun 2017 A1
20170172442 Govari Jun 2017 A1
20170185702 Auerbach et al. Jun 2017 A1
20170202515 Zrihem et al. Jul 2017 A1
20170221262 Laughner et al. Aug 2017 A1
20170224958 Cummings et al. Aug 2017 A1
20170265812 Williams et al. Sep 2017 A1
20170281031 Houben et al. Oct 2017 A1
20170281268 Tran et al. Oct 2017 A1
20170296125 Altmann et al. Oct 2017 A1
20170296251 Wu et al. Oct 2017 A1
20170311829 Beeckler et al. Nov 2017 A1
20170311893 Beeckler et al. Nov 2017 A1
20170312022 Beeckler et al. Nov 2017 A1
20170347896 Keyes et al. Dec 2017 A1
20170347959 Guta et al. Dec 2017 A1
20170354338 Levin et al. Dec 2017 A1
20170354339 Zeidan et al. Dec 2017 A1
20170354364 Bar-Tal et al. Dec 2017 A1
20180000420 Romanowski et al. Jan 2018 A1
20180008203 Iyun et al. Jan 2018 A1
20180028084 Williams et al. Feb 2018 A1
20180049803 Solis Feb 2018 A1
20180074693 Jones et al. Mar 2018 A1
20180085064 Auerbach et al. Mar 2018 A1
20180110562 Govari et al. Apr 2018 A1
20180125575 Schwartz et al. May 2018 A1
20180132749 Govari et al. May 2018 A1
20180137687 Katz et al. May 2018 A1
20180160936 Govari et al. Jun 2018 A1
20180160978 Cohen et al. Jun 2018 A1
20180168511 Hall et al. Jun 2018 A1
20180184982 Basu et al. Jul 2018 A1
20180192958 Wu Jul 2018 A1
20180206792 Auerbach et al. Jul 2018 A1
20180235692 Efimov et al. Aug 2018 A1
20180249959 Osypka Sep 2018 A1
20180256109 Wu et al. Sep 2018 A1
20180256247 Govari et al. Sep 2018 A1
20180279954 Hayam et al. Oct 2018 A1
20180280080 Govari et al. Oct 2018 A1
20180296114 Welsh et al. Oct 2018 A1
20180303414 Toth et al. Oct 2018 A1
20180310987 Altmann et al. Nov 2018 A1
20180311497 Viswanathan et al. Nov 2018 A1
20180333162 Saab Nov 2018 A1
20180338722 Altmann et al. Nov 2018 A1
20180344188 Govari Dec 2018 A1
20180344202 Bar-Tal et al. Dec 2018 A1
20180344251 Harlev et al. Dec 2018 A1
20180344393 Gruba et al. Dec 2018 A1
20180360534 Teplitsky et al. Dec 2018 A1
20180365355 Auerbach et al. Dec 2018 A1
20180368927 Lyons et al. Dec 2018 A1
20190000540 Cohen et al. Jan 2019 A1
20190008582 Govari et al. Jan 2019 A1
20190015007 Rottmann et al. Jan 2019 A1
20190030328 Stewart et al. Jan 2019 A1
20190053708 Gliner Feb 2019 A1
20190059766 Houben et al. Feb 2019 A1
20190059818 Herrera et al. Feb 2019 A1
20190060622 Beeckler Feb 2019 A1
20190069950 Viswanathan et al. Mar 2019 A1
20190069954 Cohen et al. Mar 2019 A1
20190117111 Osadchy et al. Apr 2019 A1
20190117303 Claude et al. Apr 2019 A1
20190117315 Keyes et al. Apr 2019 A1
20190125439 Rohl et al. May 2019 A1
20190133552 Shemesh et al. May 2019 A1
20190142293 Solis May 2019 A1
20190143079 Beeckler et al. May 2019 A1
20190164633 Ingel et al. May 2019 A1
20190167137 Bar-Tal et al. Jun 2019 A1
20190167140 Williams et al. Jun 2019 A1
20190175262 Govari et al. Jun 2019 A1
20190175263 Altmann et al. Jun 2019 A1
20190183567 Govari et al. Jun 2019 A1
20190188909 Yellin et al. Jun 2019 A1
20190201664 Govari Jul 2019 A1
20190201669 Govari et al. Jul 2019 A1
20190209089 Baram et al. Jul 2019 A1
20190216346 Ghodrati et al. Jul 2019 A1
20190216347 Ghodrati et al. Jul 2019 A1
20190217065 Govari et al. Jul 2019 A1
20190231421 Viswanathan et al. Aug 2019 A1
20190231423 Weinkam et al. Aug 2019 A1
20190239811 Just et al. Aug 2019 A1
20190246935 Govari et al. Aug 2019 A1
20190297441 Dehe et al. Sep 2019 A1
20190298441 Clark et al. Oct 2019 A1
20190298442 Ogata et al. Oct 2019 A1
20190314083 Herrera et al. Oct 2019 A1
20190328260 Zeidan et al. Oct 2019 A1
20190343580 Nguyen et al. Nov 2019 A1
20190365451 Jung, Jr. Dec 2019 A1
20200000518 Kiernan et al. Jan 2020 A1
20200001054 Jimenez et al. Jan 2020 A1
20200008705 Ziv-Ari et al. Jan 2020 A1
20200008869 Byrd Jan 2020 A1
20200009378 Stewart et al. Jan 2020 A1
20200015693 Beeckler et al. Jan 2020 A1
20200015890 To et al. Jan 2020 A1
20200022653 Moisa Jan 2020 A1
20200029845 Baram et al. Jan 2020 A1
20200046421 Govari Feb 2020 A1
20200046423 Viswanathan et al. Feb 2020 A1
20200060569 Tegg Feb 2020 A1
20200077959 Altmann et al. Mar 2020 A1
20200085497 Zhang et al. Mar 2020 A1
20200093539 Long et al. Mar 2020 A1
20200129089 Gliner et al. Apr 2020 A1
20200129125 Govari et al. Apr 2020 A1
20200129128 Gliner et al. Apr 2020 A1
20200155226 Valls et al. May 2020 A1
20200163707 Sliwa et al. May 2020 A1
20200179650 Beeckler et al. Jun 2020 A1
20200196896 Solis Jun 2020 A1
20200205689 Squires et al. Jul 2020 A1
20200205690 Williams et al. Jul 2020 A1
20200205737 Beeckler Jul 2020 A1
20200205876 Govari Jul 2020 A1
20200205892 Viswanathan et al. Jul 2020 A1
20200206461 Govari et al. Jul 2020 A1
20200206498 Arora et al. Jul 2020 A1
20200289197 Viswanathan et al. Sep 2020 A1
20200297234 Houben et al. Sep 2020 A1
20200297281 Basu et al. Sep 2020 A1
20200305726 Salvestro et al. Oct 2020 A1
20200305946 DeSimone et al. Oct 2020 A1
20200397328 Altmann et al. Dec 2020 A1
20200398048 Krimsky et al. Dec 2020 A1
20210015549 Haghighi-Mood et al. Jan 2021 A1
20210022684 Govari et al. Jan 2021 A1
20210045805 Govari et al. Feb 2021 A1
20210059549 Urman et al. Mar 2021 A1
20210059550 Urman et al. Mar 2021 A1
20210059608 Beeckler et al. Mar 2021 A1
20210059743 Govari Mar 2021 A1
20210059747 Krans et al. Mar 2021 A1
20210077184 Basu et al. Mar 2021 A1
20210082157 Rosenberg et al. Mar 2021 A1
20210085200 Auerbach et al. Mar 2021 A1
20210085204 Auerbach et al. Mar 2021 A1
20210085215 Auerbach et al. Mar 2021 A1
20210085387 Amit et al. Mar 2021 A1
20210093292 Baram et al. Apr 2021 A1
20210093294 Shemesh et al. Apr 2021 A1
20210093374 Govari et al. Apr 2021 A1
20210093377 Herrera et al. Apr 2021 A1
20210100612 Baron et al. Apr 2021 A1
20210113822 Beeckler et al. Apr 2021 A1
20210127999 Govari et al. May 2021 A1
20210128010 Govari et al. May 2021 A1
20210133516 Govari et al. May 2021 A1
20210169421 Govari Jun 2021 A1
20210169567 Govari et al. Jun 2021 A1
20210169568 Govari et al. Jun 2021 A1
20210177294 Gliner et al. Jun 2021 A1
20210177356 Gliner et al. Jun 2021 A1
20210178166 Govari et al. Jun 2021 A1
20210186363 Gliner et al. Jun 2021 A1
20210187241 Govari et al. Jun 2021 A1
20210196372 Altmann et al. Jul 2021 A1
20210196394 Govari et al. Jul 2021 A1
20210212591 Govari et al. Jul 2021 A1
20210219904 Yarnitsky et al. Jul 2021 A1
20210278936 Katz et al. Sep 2021 A1
20210282659 Govari et al. Sep 2021 A1
20210307815 Govari et al. Oct 2021 A1
20210308424 Beeckler et al. Oct 2021 A1
20210338319 Govari et al. Nov 2021 A1
Foreign Referenced Citations (125)
Number Date Country
101088459 Dec 2007 CN
101384214 Mar 2009 CN
101422637 May 2009 CN
101766502 Jul 2010 CN
102271607 Dec 2011 CN
102458566 May 2012 CN
103732132 Apr 2014 CN
203539434 Apr 2014 CN
103860264 Jun 2014 CN
104244856 Dec 2014 CN
10456117 Apr 2015 CN
104783892 Jul 2015 CN
104812297 Jul 2015 CN
104887294 Sep 2015 CN
104936509 Sep 2015 CN
105105844 Dec 2015 CN
204814163 Dec 2015 CN
105473091 Apr 2016 CN
105473093 Apr 2016 CN
111248993 Jun 2020 CN
111248996 Jun 2020 CN
0668740 Aug 1995 EP
0779059 Jun 1997 EP
0644738 Mar 2000 EP
0727183 Nov 2002 EP
0727184 Dec 2002 EP
1790304 May 2007 EP
2682157 Jan 2014 EP
2749214 Jul 2014 EP
2783651 Oct 2014 EP
28665350 Apr 2015 EP
2875790 May 2015 EP
2699151 Nov 2015 EP
2699152 Nov 2015 EP
2699153 Dec 2015 EP
2498706 Apr 2016 EP
2578173 Jun 2017 EP
3238645 Nov 2017 EP
3238646 Nov 2017 EP
3238648 Nov 2017 EP
3251622 Dec 2017 EP
2884931 Jan 2018 EP
3300680 Apr 2018 EP
3315087 May 2018 EP
3332727 Jun 2018 EP
2349440 Aug 2019 EP
3571983 Nov 2019 EP
3318211 Dec 2019 EP
3581135 Dec 2019 EP
3586778 Jan 2020 EP
2736434 Feb 2020 EP
3451962 Mar 2020 EP
3653153 May 2020 EP
3972510 Mar 2022 EP
H06205837 Jul 1994 JP
H1176183 Mar 1999 JP
H1176233 Mar 1999 JP
H06261951 Mar 1999 JP
2000504242 Apr 2000 JP
2002345765 Dec 2002 JP
2005052424 Mar 2005 JP
2005525162 Aug 2005 JP
2006511296 Apr 2006 JP
2008508064 Mar 2008 JP
2010507404 Mar 2010 JP
2010522623 Jul 2010 JP
2011500172 Jan 2011 JP
2011152430 Aug 2011 JP
2012024156 Feb 2012 JP
2013013726 Jan 2013 JP
2013078587 May 2013 JP
2013529109 Jul 2013 JP
2013531525 Aug 2013 JP
2014506171 Mar 2014 JP
2014507197 Mar 2014 JP
2014529419 Nov 2014 JP
2014530039 Nov 2014 JP
2015503365 Feb 2015 JP
2015100706 Jun 2015 JP
2015112113 Jun 2015 JP
2015112114 Jun 2015 JP
2015134166 Jul 2015 JP
2015518776 Jul 2015 JP
2015139707 Aug 2015 JP
2015167864 Sep 2015 JP
2016515442 May 2016 JP
2016116863 Jun 2016 JP
9421167 Sep 1994 WO
9421169 Sep 1994 WO
9625095 Aug 1996 WO
9634560 Nov 1996 WO
0053237 Sep 2000 WO
0182814 Nov 2001 WO
02102231 Dec 2002 WO
2004087249 Oct 2004 WO
22005041748 May 2005 WO
2008049087 Apr 2008 WO
2011143468 Nov 2011 WO
2012092016 Jul 2012 WO
2012100185 Jul 2012 WO
2013049601 Apr 2013 WO
2013052852 Apr 2013 WO
2013052919 Apr 2013 WO
2013154776 Oct 2013 WO
2013162884 Oct 2013 WO
2013173917 Nov 2013 WO
2013176881 Nov 2013 WO
2014168987 Oct 2014 WO
2014176205 Oct 2014 WO
2015049784 Apr 2015 WO
2016019760 Feb 2016 WO
2016044687 Mar 2016 WO
2016183337 Nov 2016 WO
2016210437 Dec 2016 WO
2017024306 Feb 2017 WO
2017087549 May 2017 WO
2018106569 Jun 2018 WO
2018111600 Jun 2018 WO
2018129133 Jul 2018 WO
2018191149 Oct 2018 WO
2019084442 May 2019 WO
2019095020 May 2019 WO
2019143960 Jul 2019 WO
2020026217 Feb 2020 WO
2020206328 Oct 2020 WO
Non-Patent Literature Citations (67)
Entry
Extended European Search Reporte dated Nov. 12, 2020, from corresponding EP Appl. No. 20190495.0.
First Office Action dated Apr. 6, 2021, from corresponding CN Application No. 201710433124.2.
First Office Action dated Nov. 10, 2021, from corresponding CN Application No. 201710433124.2.
First Office Action dated Nov. 10, 2021, from corresponding CN Application No. 201710433114.9.
Extended European Search Report dated Jun. 26, 2020, from corresponding EP Appl. No. 20150359.6.
Notification of Reasons for Refusal dated Jun. 1, 2021, from corresponding JP2017-113536.
Notification of Reasons for Refusal dated Jul. 6, 2021, from corresponding JP2017-113535.
Notification of Reasons for Refusal dated Feb. 22, 2022, from corresponding JP2017-113535.
Notification of Reasons for Refusal dated Mar. 15, 2022, from corresponding JP2017-113536.
Notification of Reasons for Refusal dated Aug. 30, 2022, from corresponding JP2017-113535.
Extended European Search Reporte dated Feb. 6, 2018, from corresponding EP Appl. No. 17174936.9.
Partial European Search Reporte dated Oct. 24, 2017, from corresponding EP Appl. No. 17174936.9.
European Search Reporte dated Aug. 9, 2019, from corresponding EP Appl. No. 17175072.2.
European Search Reporte dated Dec. 11, 2018, from corresponding EP Appl. No. 17175072.2.
Extended European Search Report dated Oct. 20, 2017, from corresponding EP Appl. No. 17175072.2.
Extended European Search Report dated Dec. 12, 2018, from corresponding EP Appl. No. 18192797.1.
Search Report dated Dec. 8, 2020, from corresponding CN Application No. 201710433114.
Supplementary Search Report dated Jun. 27, 2021, from corresponding CN Application No. 201710433114.
Second Office Action dated Jul. 2, 2021, from corresponding CN Application No. 201710433114.
Supplementary Search Report dated Nov. 2, 2021, from corresponding CN Application No. 201710433124.
Maury P., et al., “Three-dimensional Mapping in the Electrophysiological Laboratory,” Archives of Cardiovascular Disease, Published Jun. 7, 2018, vol. 111, pp. 456-464, https://doi.org/10.1016/j.acvd,2018,03.013, Retrieved from URL: https://www.sciencedirect.com/science/article/pii/S1875213618300901.
Article 94(3) Communication dated Aug. 9, 2019, from corresponding EP Appl. No. 17175072.2.
First Office Action dated Dec. 15, 2020, from corresponding Chinese Application No. 2017104331149.
Search Report dated May 19, 2021, from corresponding Japanese Application. No. JP2017-113536.
Search Report dated May 31, 2021, from corresponding Japanese Application. No. JP2017-113535.
Notice of Reasons for Refusal dated Jul. 6, 2021, from corresponding Japanese Application. No. JP2017-113535.
Supplemental Search from corresponding Chinese Application No. 2017104331149 dated Nov. 3, 2021.
Second Office Action dated Nov. 10, 2021, from corresponding CN Application No. 201710433124.2.
Third Office Action from corresponding Chinese Application No. 2017104331149 dated Dec. 2, 2021.
Supplementary Search from corresponding Chinese Application No. 2017104331242 dated Apr. 13, 2022.
Third Office Action dated Apr. 20, 2022, from corresponding Chinese Application No. 2017104331242.
Supplementary Search from corresponding Chinese Application No. 2017104331242 dated Jul. 5, 2022.
Fourth Office Action from corresponding Chinese Application No. 2017104331149 dated Aug. 8, 2022.
Article 94(3) communication dated Jul. 11, 2023, from corresponding European Application No. 20190495.0.
First Search from corresponding Chinese Application No. 2017104331242 dated Mar. 26, 2021.
Angela O., “AF Symposium 2017: First-in-Man Study Shows Promising Results with a Multi-Electrode Radiofrequency Balloon for Paroxysmal AF Treatment,” Cardiac Rhythm News, Jan. 20, 2017, 2 Pages, [Retrieved on Dec. 16, 2020] Retrieved from URL: https://cardiacrhythmnews.com/fist-in-man-study-shows-promising-results-with-a-multi-electrode-radiofrequency-balloon-for-paroxysmal-af-treatment/.
Casella M., et al., “Ablation Index as a Predictor of Long-Term Efficacy in Premature Ventricular Complex Ablation: A Regional Target Value Analysis,” Heart Rhythm Society, Jun. 2019, vol. 16, No. 6, pp. 888-895.
Co-Pending U.S. Appl. No. 14/578,807, filed Dec. 22, 2014, 21 pages.
Das M., et al., “Ablation Index, a Novel Marker of Ablation Lesion Quality: Prediction of Pulmonary Vein Reconnection at Repeat Electrophysiology Study and Regional Differences in Target Values,” Europace, 2017, Published Online May 31, 2016, vol. 19, pp. 775-783.
Dorobantu M., et al., “Oral Anticoagulation During Atrial Fibrillation Ablation: Facts and Controversies,” Cor et Vasa, 2013, Accepted on Dec. 3, 2012, vol. 55, No.2, pp. e101-e106, Retrieved from URL: https://www.sciencedirect.com/science/article/pii/s0010865012001415.
Extended European Search Report for Application No. EP17168513.4 mailed Sep. 18, 2017, 11 pages.
Extended European Search Report for European Application No. 15201723.2, mailed May 11, 2016, 7 pages.
Extended European Search Report for European Application No. 17168393.1 mailed Dec. 15, 2017, 12 Pages.
Extended European Search Report for European Application No. 17168518.3, mailed Sep. 20, 2017, 9 Pages.
Extended European Search Report for European Application No. 17173893.3, mailed Nov. 6, 2017, 8 Pages.
Extended European Search Report for European Application No. 17201434.2, mailed Feb. 1, 2018, 10 Pages.
Extended European Search Report for European Application No. 17205876.0, mailed Jun. 1, 2018, 13 Pages.
Extended European Search Report for European Application No. 19177365.4, mailed Nov. 8, 2019, 07 Pages.
Extended European Search Report for European Application No. 19183327.6, mailed Nov. 21, 2019, 8 Pages.
Extended European Search Report for European Application No. 20153872.5, mailed May 7, 2020, 9 Pages.
Extended European Search Report for European Application No. 20195648.9, mailed Feb. 12, 2021, 9 Pages.
Fornell D., “Multi-Electrode RF Balloon Efficient for Acute Pulmonary Vein Isolation,” Diagnostic and Interventional Cardiology, May 17, 2017, 3 Pages, [Retrieved on Dec. 16, 2020] Retrieved from URL: www.dicardiology.com/article/multi-electrode-rf-balloon-efficient-acute-pulmonary-vein-isolation.
Haines D.E., et al., “The Promise of Pulsed Field Ablation,” Dec. 2019, vol. 19, No. 12, 10 Pages.
Honarbakhsh S., et al., “Radiofrequency Balloon Catheter Ablation for Paroxysmal Atrial Fibrillation, Radiance Study—a UK experience,” EP Europace, Oct. 2017, vol. 19, No. 1, p. i21, 3 Pages.
International Search Report and Written Opinion for International Application No. PCT/IB2019/052313, mailed Jul. 22, 2019, 8 Pages.
International Search Report and Written Opinion for International Application No. PCT/IB2019/056381, mailed Dec. 17, 2019, 10 Pages.
International Search Report and Written Opinion for International Application No. PCT/IB2019/057743, mailed Dec. 6, 2019, 16 Pages.
International Search Report and Written Opinion issued in corresponding International Application No. PCT/IB2019/057742, dated Nov. 28, 2019, 18 Pages.
Nagashima K., et al., “Hot Balloon Versus Cryoballoon Ablation for Atrial Fibrillation,” Circulation: Arrhythmia and Electrophysiology, May 2018, Vol. 11, No. 5, e005861, 9 Pages.
Napoli N., et al., “For Atrial Fibrillation Abalation, Newer Anticoagulant Reduces Major Bleeds,” American Collage of Cardiology, Mar. 19, 2017, 4 Pages, [Retrieved on Jan 1, 2022] Retrieved from URL: http://www.acc.org/about-acc/press-releases/2017/03/18/08/47/sun-1045am-for-atrial-fibrillation-ablation-newer-anticoagulant-reduces-major-bleeds.
Okano T., et al., “Wire Perforation Causing Cardiopulmonary Arrest During Radiofrequency Hot Balloon Ablation for Pulmonary Vein Isolation,”Journal of Cardiology Cases, Feb. 15, 2019, vol. 19, No. 5, pp. 169-172.
Partial European Search Report for European Application No. 17168393.1 mailed Sep. 13, 2017, 13 Pages.
Partial European Search Report for European Application No. 17205876.0, mailed Feb. 22, 2018, 10 Pages.
Reddy V.Y., et al., “Ballon Catherer Ablation to Treat Proxysmal Atrial Fibrillation: What is the Level of Pulmonary Venous Isolation?,” Heart Rhythm, Mar. 2008, vol. 5, No. 3, pp. 353-360, 3 Pages.
Winkle R.A., et al., “Atrial Fibrillation Ablation Using Open-Irrigated Tip Radiofrequency: Experience with Intraprocedural Activated Clotting Times ≤ 210 Seconds,” Heart Rhythm, Jun. 2014, Epub Mar. 27, 2014, vol. 11. No. 6, pp. 963-968.
Youtube:, “Intensity™ CX4 Professional E-Stim/ Ultrasound Combo,” Dec. 22, 2015, 1 Page, [Retrieved on Nov. 19, 2020], Retrieved from URL: http://www.youtube.com/watch?v=76s1QkMWJME].
Youtube: “New Interface TactiCath Contact Force Ablation Catheter,”Nov. 26, 2013, 1 Pages, [Retrieved on Nov. 19, 2020], Retrieved from URL: https: /Avww.youtube.com/watch?v=aTvYO8Hpylg].
Related Publications (1)
Number Date Country
20210145282 A1 May 2021 US
Continuations (1)
Number Date Country
Parent 15359838 Nov 2016 US
Child 17163096 US
Continuation in Parts (1)
Number Date Country
Parent 15177775 Jun 2016 US
Child 15359838 US